Variant #0000011649 (NC_000001.10:-, NMNAT1(NM_022787.3):c.507G>A)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
NMNAT1_00001 See all 4 reported entries |
Frequency |
- |
Variant remarks |
It is inherited from father who carry the mutation p.Trp169X.
There are three members in this family. The son is the patient and has mutations p.W169X and p.E257K. The parents are normal. The mother only carries the mutation p.E257K. The father carries the mutation p.W169X. |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
|
|